Electrocatalytic enhancement of formic acid oxidation reaction by acetonitrile on well-defined platinum surfaces

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10045/83609
Registro completo de metadatos
Registro completo de metadatos
Campo DCValorIdioma
dc.contributorElectroquímica de Superficieses_ES
dc.contributorElectroquímica Aplicada y Electrocatálisises_ES
dc.contributor.authorBriega-Martos, Valentín-
dc.contributor.authorSolla-Gullón, José-
dc.contributor.authorKoper, Marc T.M.-
dc.contributor.authorHerrero, Enrique-
dc.contributor.authorFeliu, Juan M.-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Físicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Electroquímicaes_ES
dc.date.accessioned2018-11-15T10:57:57Z-
dc.date.available2018-11-15T10:57:57Z-
dc.date.issued2019-02-01-
dc.identifier.citationElectrochimica Acta. 2019, 295: 835-845. doi:10.1016/j.electacta.2018.11.016es_ES
dc.identifier.issn0013-4686 (Print)-
dc.identifier.issn1873-3859 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/83609-
dc.description.abstractThe formic acid oxidation reaction has been studied on Pt(111), Pt(100) and Pt nanoparticles with preferential (111) surface structure in 0.1 M HClO4 in the presence of different concentrations of acetonitrile. An electrocatalytic enhancement towards the formic acid oxidation has been observed under these conditions, and it is proposed that this enhancement is due to two different effects of the adsorbed acetonitrile species: a third-body effect which hinders the formation of CO and a promoting effect of the direct oxidation of formic acid. This promoting effect is structure sensitive. The different enhancement between Pt(111) and Pt(100) indicates that the ratio of free Pt sites and sites occupied by adsorbed acetonitrile is important in order to have the better electrocatalytic activity. On-line mass spectrometry (OLEMS) measurements confirmed the preference for the direct oxidation of formic acid to CO2, which is almost complete below 0.3 V vs. RHE for Pt(111). Finally, chronoamperometric studies confirmed the lower poisoning rate in the presence of acetonitrile but they also pointed out a competition of formed CO for the Pt sites occupied by acetonitrile species. This work constitutes an example of electrocatalytic enhancement by using an organic molecule for surface modification, which is not as common as using metallic adlayers.es_ES
dc.description.sponsorshipThis work has been financially supported by the MINECO-FEDER (Spain) through project CTQ2016-76221-P. V. B-M thankfully acknowledges to MINECO the award of a predoctoral grant (BES-2014-068176, project CTQ2013-44803-P) and a student stay grant (EEBB-I-16-11656). S-G. acknowledges financial support from Vicerrectorado de Investigación y Transferencia de Conocimiento of the University of Alicante (UATALENTO16-02).es_ES
dc.languageenges_ES
dc.publisherElsevieres_ES
dc.rights© 2018 Elsevier Ltd.es_ES
dc.subjectFormic acid oxidationes_ES
dc.subjectPlatinum single crystal electrodeses_ES
dc.subjectAcetonitrilees_ES
dc.subjectElectrocatalysises_ES
dc.subject.otherQuímica Físicaes_ES
dc.titleElectrocatalytic enhancement of formic acid oxidation reaction by acetonitrile on well-defined platinum surfaceses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1016/j.electacta.2018.11.016-
dc.relation.publisherversionhttps://doi.org/10.1016/j.electacta.2018.11.016es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
Aparece en las colecciones:INV - LEQA - Artículos de Revistas
INV - EQSUP - Artículos de Revistas

Archivos en este ítem:
Archivos en este ítem:
Archivo Descripción TamañoFormato 
Thumbnail2019_Briega-Martos_etal_ElectActa_final.pdfVersión final (acceso restringido)1,14 MBAdobe PDFAbrir    Solicitar una copia
Thumbnail2019_Briega-Martos_etal_ElectActa_accepted.pdfAccepted Manuscript (acceso abierto)818,52 kBAdobe PDFAbrir Vista previa


Todos los documentos en RUA están protegidos por derechos de autor. Algunos derechos reservados.